A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10587637



Internal ID5924865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:95236825..95253706hg38UCSC Ensembl
chr2:95902573..95919454hg19UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg3816882
hg1916882
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3591665
Supporting Variants
SamplesNA19332
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10587637
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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